Canonical Allele Identifier: CA2693251441
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359801_19359860del , CM000685.2:g.19359801_19359860del GRCh38
NC_000023.10:g.19377919_19377978del , CM000685.1:g.19377919_19377978del GRCh37
NC_000023.9:g.19287840_19287899del NCBI36
NG_016781.1:g.20909_20968del
NG_021184.1:g.160402_160461del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*148_*207del ENSP00000348062.6:n.*148_*207del
ENST00000423505.6:c.*148_*207del ENSP00000406473.2:n.*148_*207del
ENST00000696704.1:c.*653_*712del ENSP00000512823.1:n.*653_*712del
ENST00000696705.1:c.*776_*835del ENSP00000512824.1:n.*776_*835del
ENST00000422285.7:c.*148_*207del MANE Select ENSP00000394382.2:n.*148_*207del
ENST00000379806.9:c.*148_*207del ENSP00000369134.5:n.*148_*207del
ENST00000422285.6:c.*148_*207del ENSP00000394382.2:n.*148_*207del
ENST00000540249.5:c.*148_*207del ENSP00000440761.1:n.*148_*207del
ENST00000545074.5:c.*148_*207del ENSP00000438550.1:n.*148_*207del
NM_000284.3:c.*148_*207del NP_000275.1:n.*148_*207del
NM_001173454.1:c.*148_*207del NP_001166925.1:n.*148_*207del
NM_001173455.1:c.*148_*207del NP_001166926.1:n.*148_*207del
NM_001173456.1:c.*148_*207del NP_001166927.1:n.*148_*207del
XM_011545531.1:c.*148_*207del XP_011543833.1:n.*148_*207del
XM_011545532.1:c.*148_*207del XP_011543834.1:n.*148_*207del
NM_000284.4:c.*148_*207del MANE Select NP_000275.1:n.*148_*207del
NM_001173454.2:c.*148_*207del NP_001166925.1:n.*148_*207del
NM_001173455.2:c.*148_*207del NP_001166926.1:n.*148_*207del
NM_001173456.2:c.*148_*207del NP_001166927.1:n.*148_*207del